A Novel Approach to α‐Arylacetonitrile Skeletons via para‐Selective Alkylation of Protected Anilines

Abstract

AbstractA ruthenium‐catalyzed para‐selective alkylation of protected anilines to construct α‐arylacetonitrile skeletons has been reported. We firstly disclosed the ethyl 2‐bromo‐2‐cyanopropanoate was an effective alkylating reagent in ruthenmuim‐catalyzed remote‐selective C−H functionalization. A wide variety of α‐arylacetonitrile skeletons can be directly obtained with moderate to good yields. Importantly, the products contain both nitrile and ester groups guaranteeing its direct transformation into other useful synthetic units, indicating the synthetic importance of this method.